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Links from GEO DataSets

Items: 20

1.

Conversion of human fibroblasts into vascular cells

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array; Expression profiling by array
Platforms:
GPL6947 GPL13534 GPL10558
50 Samples
Download data
Series
Accession:
GSE40927
ID:
200040927
2.

Conversion of human fibroblasts into vascular cells (methylation)

(Submitter supplied) We report a novel technique to reprogram human fibroblasts into endothelial and smooth muscle cells using partial iPSC reprogramming and chemically defined media. Using appropriate media conditions for differentiation of human pluripotent cells to CD34+ vascular progenitor cells, we show that temporary expression of pluripotent transcription factors and treatment with chemically-defined media, will induce differentiation of human fibroblasts to CD34+ vascular progenitor cells. more...
Organism:
Homo sapiens
Type:
Methylation profiling by genome tiling array
Platform:
GPL13534
25 Samples
Download data: TXT
Series
Accession:
GSE40909
ID:
200040909
3.

Conversion of human fibroblasts into vascular cells (gene expression)

(Submitter supplied) We report a novel technique to reprogram human fibroblasts into endothelial and smooth muscle cells using partial iPSC reprogramming and chemically defined media. Using appropriate media conditions for differentiation of human pluripotent cells to CD34+ vascular progenitor cells, we show that temporary expression of pluripotent transcription factors and treatment with chemically-defined media, will induce differentiation of human fibroblasts to CD34+ vascular progenitor cells. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL10558 GPL6947
25 Samples
Download data: TXT
Series
Accession:
GSE40793
ID:
200040793
4.

A novel reprogramming strategy to generate functionally competent human hepatocytes

(Submitter supplied) Cell fate can be directly converted between differentiated cells by lineage reprogramming, thus generating multiple cell types across developmental lineages. However, lineage reprogramming is hindered by incomplete cell-fate conversion with residual initial cell identity and partial functions compared with the native counterparts. Here, we develop a high-fidelity reprogramming strategy, by mimicking the natural cell-fate changing route, thus permitting the production of functionally competent human hepatocytes from another cell type. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
Platforms:
GPL20301 GPL16791
47 Samples
Download data: CSV
5.

Molecular profiling of human mammary gland links breast cancer risk to a p27+ cell population with progenitor characteristics

(Submitter supplied) Gene expression, DNA and histone methylation profiles were performed on multiple cell types purified from normal human nulliparous and parous breast tissue using SAGE-seq, MSDK-seq and ChIP-seq [GSE26141].
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platform:
GPL9052
42 Samples
Download data: TXT
Series
Accession:
GSE32017
ID:
200032017
6.

Tet and TDG Mediate DNA Demethylation Essential for MET in Somatic Cell Reprogramming

(Submitter supplied) Tet-mediated DNA oxidation is a new type of epigenetic modification in mammals and its role in the regulation of cell fate transition remains poorly understood. Here, we derive mouse embryonic fibroblasts (MEFs) deleted in all three Tet genes and examine their capability to be reprogrammed into iPS cells. We demonstrate that these Tet-deficient MEFs cannot be reprogrammed due to a blockage in the mesenchymal-to-epithelial transition (MET). more...
Organism:
Mus musculus
Type:
Methylation profiling by high throughput sequencing
Platform:
GPL13112
4 Samples
Download data: WIG
Series
Accession:
GSE52741
ID:
200052741
7.

Intrinsic differentiation potential of human postnatal MSC, Mab and MAPC reflected in their transcriptome

(Submitter supplied) We have employed whole genome microarray expression profiling to identify genes that characterize different populations of human postnatal stem cells and reflect their potency
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
31 Samples
Download data: TXT
Series
Accession:
GSE23131
ID:
200023131
8.

Growth factor-activated stem cell circuits and stromal signals cooperatively accelerate iPSC reprogramming of lineage-committed myeloid progenitors

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL6947 GPL10558
47 Samples
Download data
Series
Accession:
GSE35029
ID:
200035029
9.

Global gene expression analysis of pluripotent cell lines and corresponding starting donor source cells

(Submitter supplied) Global gene expression analysis of induced pluripotent stem cell lines and their corresponding source cells
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6947
17 Samples
Download data: TXT
Series
Accession:
GSE35028
ID:
200035028
10.

Global gene expression analysis of human embryonic stem cells, adult fibroblasts , and CD34+ cord blood (CB) cells before, during, and afer their episomal induction of pluripotency

(Submitter supplied) Global gene expression analysis of (a) human embryonic stem cells, (b) adult fibroblasts with and without nucleofection of SOKM, and ( c ) CD34+ cord blood cells at various time points during induction of pluripotency with SOKM, with or without co-culture with bone marrow stromal cells (BMSC).
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
30 Samples
Download data: TXT
Series
Accession:
GSE35027
ID:
200035027
11.

Direct reprogramming of human fibroblasts to functional hepatocyte-like cells

(Submitter supplied) Plasticity of differentiated cells has been proved by nuclear transfer, induced pluripotent cells and transdifferentiation. Here we show that by transduction of 3 factors (FOXA3, HNF1A and HNF4A), human fetal fibroblasts can be converted to hepatocyte-like cells (hiHep cells), expressing hepatic marker genes, and acquiring many mature hepatocyte functions in vitro and in vivo.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL4133
13 Samples
Download data: TXT
Series
Accession:
GSE42643
ID:
200042643
12.

Direct reprogramming of mouse fibroblasts into functional skeletal muscle progenitors

(Submitter supplied) Skeletal muscle harbors quiescent stem cells termed satellite cells and proliferative progenitors termed myoblasts, which play pivotal roles during muscle regeneration. However, current technology does not allow permanent capture of these cell populations in vitro. Here, we show that ectopic expression of the myogenic transcription factor MyoD, combined with exposure to small molecules, reprograms mouse fibroblasts into expandable induced myogenic progenitor cells (iMPCs). more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13112
6 Samples
Download data: BW, TXT
Series
Accession:
GSE108543
ID:
200108543
13.

Direct reprogramming of mouse fibroblasts into functional skeletal muscle progenitors

(Submitter supplied) Skeletal muscle harbors quiescent stem cells termed satellite cells and proliferative progenitors termed myoblasts, which play pivotal roles during muscle regeneration. However, current technology does not allow permanent capture of these cell populations in vitro. Here, we show that ectopic expression of the myogenic transcription factor MyoD, combined with exposure to small molecules, reprograms mouse fibroblasts into expandable induced myogenic progenitor cells (iMPCs). more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL16570
5 Samples
Download data: CEL
Series
Accession:
GSE92336
ID:
200092336
14.

Notch-HES1 signaling axis controls hemato-endothelial fate decisions of human embyronic and induced pluripotent cells

(Submitter supplied) Notch signaling regulates several cellular processes including cell fate decisions and proliferation in both invertebrates and mice. However, comparatively less is known about the role of Notch during early human development. Here, we examined the function of Notch signaling during hematopoietic lineage specification from human pluripotent stem cells (hPSCs) of both embryonic and adult fibroblast origin. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
8 Samples
Download data: CEL
Series
Accession:
GSE47466
ID:
200047466
15.

Small molecule-mediated reprogramming of human hepatocytes into bipotent progenitor cells

(Submitter supplied) Currently, much effort is directed to the development of new cell sources for clinical therapy using cell fate conversion approaches by small molecules. Direct lineage reprogramming to a progenitor state has been reported in terminally differentiated rodent hepatocytes, yet remains a challenge in human hepatocytes. Human hepatocytes were isolated from healthy and diseased donor livers and reprogrammed into progenitor cells by two small molecules, A83-01 and CHIR99021 (AC), in the presence of EGF and HGF. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
7 Samples
Download data: TXT
Series
Accession:
GSE114643
ID:
200114643
16.

Generation of intestinal progenitor cells from mouse fibroblasts

(Submitter supplied) We show direct conversion of mouse fibroblasts to cells that closely resemble intestinal stem cells (ISCs), through the state of fetal-type progenitor cells, called FIPCs. The induced ISCs (iISCs) exhibit self-renewal capacity and intestinal multi-lineage differentiation potential. Upon transplantation, iFIPCs and iISCs reconstitute colonic and intestinal epithelia, respectively.
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL7202
18 Samples
Download data: TXT
Series
Accession:
GSE85232
ID:
200085232
17.

Lineage Reprogramming of Fibroblasts into Functional Neurons and Hepatocytes via Chemically Induced XEN-like State

(Submitter supplied) Small-molecule based lineage reprogramming has newly emerged as a promising approach for generating functional cell types. We recently found that the chemical induction of iPSCs from fibroblasts pass through an extra-embryonic endoderm (XEN)-like state. In this study, we demonstrated that these chemically-induced XEN-like cells were not restricted to be reprogrammed to iPSCs, but feasible to be induced into functional neurons, bypassing the pluripotent stage. more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21273
34 Samples
Download data: XLS
Series
Accession:
GSE97721
ID:
200097721
18.

Chemical induction of liver progenitor cells from mature hepatocytes

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Rattus norvegicus; Mus musculus
Type:
Expression profiling by array
Platforms:
GPL15084 GPL21163
96 Samples
Download data: TXT
Series
Accession:
GSE87764
ID:
200087764
19.

Conversion of terminally committed hepatocytes to culturable bipotent progenitor cells with regenerative capacity

(Submitter supplied) A challenge for advancing approaches to liver regeneration is loss of functional differentiation capacity when hepatocyte progenitors are maintained in culture. Recent lineage-tracing studies have shown that mature hepatocytes (MHs) convert to an immature state during chronic liver injury, and we investigated whether this conversion could be recapitulated in vitro and if such converted cells could represent a source of expandable hepatocytes. more...
Organism:
Rattus norvegicus
Type:
Expression profiling by array
Platform:
GPL15084
75 Samples
Download data: TXT
Series
Accession:
GSE87611
ID:
200087611
20.

Conversion of terminally committed mouse hepatocytes to culturable bipotent progenitor cells

(Submitter supplied) A challenge for advancing approaches to liver regeneration is loss of functional differentiation capacity when hepatocyte progenitors are maintained in culture. Recent lineage-tracing studies have shown that mature hepatocytes (MHs) convert to an immature state during chronic liver injury, and we investigated whether this conversion could be recapitulated in vitro and if such converted cells could represent a source of expandable hepatocytes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL21163
21 Samples
Download data: TXT
Series
Accession:
GSE87579
ID:
200087579
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